ISOLATION, CHARACTERIZATION, AND EXPRESSION OF THE MURINE WILMS-TUMOR GENE (WT1) DURING KIDNEY DEVELOPMENT

被引:245
作者
BUCKLER, AJ
PELLETIER, J
HABER, DA
GLASER, T
HOUSMAN, DE
机构
[1] MIT,CTR CANC RES,CAMBRIDGE,MA 02139
[2] MASSACHUSETTS GEN HOSP,CTR CANC,BOSTON,MA 02114
[3] HARVARD UNIV,SCH MED,BOSTON,MA 02115
关键词
D O I
10.1128/MCB.11.3.1707
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human Wilms' tumor predisposition gene, WT1, is a Cys-His zinc finger polypeptide which appears to be a transcription factor controlling gene expression during embryonic kidney development. In order to analyze the role of the WT1 gene in nephroblast differentiation, we have isolated the murine homolog of human WT1. An extremely high level of amino acid sequence conservation (> 95%) extends throughout all regions of the predicted mouse and human WT1 polypeptides. Two alternative splices within the WT1 transcript have been conserved between mice and humans, suggesting that these have functional significance. Expression of the mouse WT1 mRNA in fetal kidney increases during late gestation, peaks just prior to or shortly after birth, and declines dramatically by 15 days postpartum. Developmental regulation of WT1 expression appears to be selective for the kidney. The restriction of WT1 expression to a limited number of tissues is in contrast to previously described tumor suppressor genes. In addition, the narrow window of time during which WT1 is expressed at high levels in the kidney is consistent with the origin of Wilms' tumor from primitive nephroblasts and the postulated role of this gene as a negative regulator of growth.
引用
收藏
页码:1707 / 1712
页数:6
相关论文
共 36 条
  • [1] AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
  • [2] GENETIC-ANALYSIS OF THE MOUSE USING INTERSPECIFIC CROSSES
    AVNER, P
    AMAR, L
    DANDOLO, L
    GUENET, JL
    [J]. TRENDS IN GENETICS, 1988, 4 (01) : 18 - 23
  • [3] STRUCTURE AND EXPRESSION OF THE MURINE RETINOBLASTOMA GENE AND CHARACTERIZATION OF ITS ENCODED PROTEIN
    BERNARDS, R
    SCHACKLEFORD, GM
    GERBER, MR
    HOROWITZ, JM
    FRIEND, SH
    SCHARTL, M
    BOGENMANN, E
    RAPAPORT, JM
    MCGEE, T
    DRYJA, TP
    WEINBERG, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) : 6474 - 6478
  • [4] BRENNER BM, 1975, KIDNEY
  • [5] ISOLATION AND CHARACTERIZATION OF A ZINC FINGER POLYPEPTIDE GENE AT THE HUMAN CHROMOSOME-11 WILMS TUMOR LOCUS
    CALL, KM
    GLASER, T
    ITO, CY
    BUCKLER, AJ
    PELLETIER, J
    HABER, DA
    ROSE, EA
    KRAL, A
    YEGER, H
    LEWIS, WH
    JONES, C
    HOUSMAN, DE
    [J]. CELL, 1990, 60 (03) : 509 - 520
  • [6] SV40 LARGE TUMOR-ANTIGEN FORMS A SPECIFIC COMPLEX WITH THE PRODUCT OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE
    DECAPRIO, JA
    LUDLOW, JW
    FIGGE, J
    SHEW, JY
    HUANG, CM
    LEE, WH
    MARSILIO, E
    PAUCHA, E
    LIVINGSTON, DM
    [J]. CELL, 1988, 54 (02) : 275 - 283
  • [7] THE HUMAN PAPILLOMA VIRUS-16 E7-ONCOPROTEIN IS ABLE TO BIND TO THE RETINOBLASTOMA GENE-PRODUCT
    DYSON, N
    HOWLEY, PM
    MUNGER, K
    HARLOW, E
    [J]. SCIENCE, 1989, 243 (4893) : 934 - 937
  • [8] HYPOMETHYLATION OF RAS ONCOGENES IN PRIMARY HUMAN CANCERS
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 111 (01) : 47 - 54
  • [9] ANIRIDIA-WILMS TUMOR ASSOCIATION - EVIDENCE FOR SPECIFIC DELETION OF 11P13
    FRANCKE, U
    HOLMES, LB
    ATKINS, L
    RICCARDI, VM
    [J]. CYTOGENETICS AND CELL GENETICS, 1979, 24 (03): : 185 - 192
  • [10] DELETIONS OF A DNA-SEQUENCE IN RETINOBLASTOMAS AND MESENCHYMAL TUMORS - ORGANIZATION OF THE SEQUENCE AND ITS ENCODED PROTEIN
    FRIEND, SH
    HOROWITZ, JM
    GERBER, MR
    WANG, XF
    BOGENMANN, E
    LI, FP
    WEINBERG, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) : 9059 - 9063